ONKI3 | Medical Subject Headings


Hierarchy:	Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Arterial Occlusive Diseases ∟ Arteriosclerosis ∟ Intracranial Arteriosclerosis ∟ Dementia, Vascular ∟ CADASIL 42 coordinate concepts ∟ Dementia, Multi-Infarct \| ∟ Cerebral Amyloid Angiopathy \| ∟ Infarction, Anterior Cerebral Artery \| ∟ Infarction, Middle Cerebral Artery \| ∟ Infarction, Posterior Cerebral Artery \| ∟ Intracranial Aneurysm \| ∟ Intracranial Arteriosclerosis \| ∟ Moyamoya Disease \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Cerebrovascular Disorders ∟ Cerebral Arterial Diseases ∟ CADASIL 42 coordinate concepts ∟ Dementia, Multi-Infarct \| ∟ Cerebral Amyloid Angiopathy \| ∟ Infarction, Anterior Cerebral Artery \| ∟ Infarction, Middle Cerebral Artery \| ∟ Infarction, Posterior Cerebral Artery \| ∟ Intracranial Aneurysm \| ∟ Intracranial Arteriosclerosis \| ∟ Moyamoya Disease \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Cerebrovascular Disorders ∟ Cerebral Arterial Diseases ∟ Intracranial Arteriosclerosis ∟ Dementia, Vascular ∟ CADASIL 42 coordinate concepts ∟ Dementia, Multi-Infarct \| ∟ Cerebral Amyloid Angiopathy \| ∟ Infarction, Anterior Cerebral Artery \| ∟ Infarction, Middle Cerebral Artery \| ∟ Infarction, Posterior Cerebral Artery \| ∟ Intracranial Aneurysm \| ∟ Intracranial Arteriosclerosis \| ∟ Moyamoya Disease \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Cerebrovascular Disorders ∟ Dementia, Vascular ∟ CADASIL 42 coordinate concepts ∟ Dementia, Multi-Infarct \| ∟ Cerebral Amyloid Angiopathy \| ∟ Infarction, Anterior Cerebral Artery \| ∟ Infarction, Middle Cerebral Artery \| ∟ Infarction, Posterior Cerebral Artery \| ∟ Intracranial Aneurysm \| ∟ Intracranial Arteriosclerosis \| ∟ Moyamoya Disease \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Cerebrovascular Disorders ∟ Intracranial Arterial Diseases ∟ Cerebral Arterial Diseases ∟ CADASIL 42 coordinate concepts ∟ Dementia, Multi-Infarct \| ∟ Cerebral Amyloid Angiopathy \| ∟ Infarction, Anterior Cerebral Artery \| ∟ Infarction, Middle Cerebral Artery \| ∟ Infarction, Posterior Cerebral Artery \| ∟ Intracranial Aneurysm \| ∟ Intracranial Arteriosclerosis \| ∟ Moyamoya Disease \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Cerebrovascular Disorders ∟ Intracranial Arterial Diseases ∟ Cerebral Arterial Diseases ∟ Intracranial Arteriosclerosis ∟ Dementia, Vascular ∟ CADASIL 42 coordinate concepts ∟ Dementia, Multi-Infarct \| ∟ Cerebral Amyloid Angiopathy \| ∟ Infarction, Anterior Cerebral Artery \| ∟ Infarction, Middle Cerebral Artery \| ∟ Infarction, Posterior Cerebral Artery \| ∟ Intracranial Aneurysm \| ∟ Intracranial Arteriosclerosis \| ∟ Moyamoya Disease \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ CADASIL 42 coordinate concepts ∟ Dementia, Multi-Infarct \| ∟ Cerebral Amyloid Angiopathy \| ∟ Infarction, Anterior Cerebral Artery \| ∟ Infarction, Middle Cerebral Artery \| ∟ Infarction, Posterior Cerebral Artery \| ∟ Intracranial Aneurysm \| ∟ Intracranial Arteriosclerosis \| ∟ Moyamoya Disease \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Mental Disorders ∟ Delirium, Dementia, Amnestic, Cognitive Disorders ∟ Dementia ∟ Dementia, Vascular ∟ CADASIL 42 coordinate concepts ∟ Dementia, Multi-Infarct \| ∟ Cerebral Amyloid Angiopathy \| ∟ Infarction, Anterior Cerebral Artery \| ∟ Infarction, Middle Cerebral Artery \| ∟ Infarction, Posterior Cerebral Artery \| ∟ Intracranial Aneurysm \| ∟ Intracranial Arteriosclerosis \| ∟ Moyamoya Disease \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Cerebrovascular Disorders ∟ Cerebral Arterial Diseases ∟ CADASIL 42 coordinate concepts ∟ Dementia, Multi-Infarct \| ∟ Cerebral Amyloid Angiopathy \| ∟ Infarction, Anterior Cerebral Artery \| ∟ Infarction, Middle Cerebral Artery \| ∟ Infarction, Posterior Cerebral Artery \| ∟ Intracranial Aneurysm \| ∟ Intracranial Arteriosclerosis \| ∟ Moyamoya Disease \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Cerebrovascular Disorders ∟ Cerebral Arterial Diseases ∟ Intracranial Arteriosclerosis ∟ Dementia, Vascular ∟ CADASIL 42 coordinate concepts ∟ Dementia, Multi-Infarct \| ∟ Cerebral Amyloid Angiopathy \| ∟ Infarction, Anterior Cerebral Artery \| ∟ Infarction, Middle Cerebral Artery \| ∟ Infarction, Posterior Cerebral Artery \| ∟ Intracranial Aneurysm \| ∟ Intracranial Arteriosclerosis \| ∟ Moyamoya Disease \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Cerebrovascular Disorders ∟ Dementia, Vascular ∟ CADASIL 42 coordinate concepts ∟ Dementia, Multi-Infarct \| ∟ Cerebral Amyloid Angiopathy \| ∟ Infarction, Anterior Cerebral Artery \| ∟ Infarction, Middle Cerebral Artery \| ∟ Infarction, Posterior Cerebral Artery \| ∟ Intracranial Aneurysm \| ∟ Intracranial Arteriosclerosis \| ∟ Moyamoya Disease \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Cerebrovascular Disorders ∟ Intracranial Arterial Diseases ∟ Cerebral Arterial Diseases ∟ CADASIL 42 coordinate concepts ∟ Dementia, Multi-Infarct \| ∟ Cerebral Amyloid Angiopathy \| ∟ Infarction, Anterior Cerebral Artery \| ∟ Infarction, Middle Cerebral Artery \| ∟ Infarction, Posterior Cerebral Artery \| ∟ Intracranial Aneurysm \| ∟ Intracranial Arteriosclerosis \| ∟ Moyamoya Disease \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Cerebrovascular Disorders ∟ Intracranial Arterial Diseases ∟ Cerebral Arterial Diseases ∟ Intracranial Arteriosclerosis ∟ Dementia, Vascular ∟ CADASIL 42 coordinate concepts ∟ Dementia, Multi-Infarct \| ∟ Cerebral Amyloid Angiopathy \| ∟ Infarction, Anterior Cerebral Artery \| ∟ Infarction, Middle Cerebral Artery \| ∟ Infarction, Posterior Cerebral Artery \| ∟ Intracranial Aneurysm \| ∟ Intracranial Arteriosclerosis \| ∟ Moyamoya Disease \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Dementia ∟ Dementia, Vascular ∟ CADASIL 42 coordinate concepts ∟ Dementia, Multi-Infarct \| ∟ Cerebral Amyloid Angiopathy \| ∟ Infarction, Anterior Cerebral Artery \| ∟ Infarction, Middle Cerebral Artery \| ∟ Infarction, Posterior Cerebral Artery \| ∟ Intracranial Aneurysm \| ∟ Intracranial Arteriosclerosis \| ∟ Moyamoya Disease \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Arterial Occlusive Diseases ∟ Arteriosclerosis ∟ Intracranial Arteriosclerosis ∟ Dementia, Vascular ∟ CADASIL Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Cerebrovascular Disorders ∟ Cerebral Arterial Diseases ∟ CADASIL Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Cerebrovascular Disorders ∟ Cerebral Arterial Diseases ∟ Intracranial Arteriosclerosis ∟ Dementia, Vascular ∟ CADASIL Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Cerebrovascular Disorders ∟ Dementia, Vascular ∟ CADASIL Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Cerebrovascular Disorders ∟ Intracranial Arterial Diseases ∟ Cerebral Arterial Diseases ∟ CADASIL Medical Subject Headings (MeSH) ∟ Cardiovascular Diseases ∟ Vascular Diseases ∟ Cerebrovascular Disorders ∟ Intracranial Arterial Diseases ∟ Cerebral Arterial Diseases ∟ Intracranial Arteriosclerosis ∟ Dementia, Vascular ∟ CADASIL Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ CADASIL Medical Subject Headings (MeSH) ∟ Mental Disorders ∟ Delirium, Dementia, Amnestic, Cognitive Disorders ∟ Dementia ∟ Dementia, Vascular ∟ CADASIL Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Cerebrovascular Disorders ∟ Cerebral Arterial Diseases ∟ CADASIL Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Cerebrovascular Disorders ∟ Cerebral Arterial Diseases ∟ Intracranial Arteriosclerosis ∟ Dementia, Vascular ∟ CADASIL Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Cerebrovascular Disorders ∟ Dementia, Vascular ∟ CADASIL Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Cerebrovascular Disorders ∟ Intracranial Arterial Diseases ∟ Cerebral Arterial Diseases ∟ CADASIL Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Cerebrovascular Disorders ∟ Intracranial Arterial Diseases ∟ Cerebral Arterial Diseases ∟ Intracranial Arteriosclerosis ∟ Dementia, Vascular ∟ CADASIL Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Dementia ∟ Dementia, Vascular ∟ CADASIL Dementia, Vascular > Intracranial Arteriosclerosis > Arteriosclerosis > Arterial Occlusive Diseases > Vascular Diseases > Cardiovascular Diseases > Medical Subject Headings (MeSH) Cerebral Arterial Diseases > Cerebrovascular Disorders > Vascular Diseases > Cardiovascular Diseases > Medical Subject Headings (MeSH) Dementia, Vascular > Intracranial Arteriosclerosis > Cerebral Arterial Diseases > Cerebrovascular Disorders > Vascular Diseases > Cardiovascular Diseases > Medical Subject Headings (MeSH) Dementia, Vascular > Cerebrovascular Disorders > Vascular Diseases > Cardiovascular Diseases > Medical Subject Headings (MeSH) Cerebral Arterial Diseases > Intracranial Arterial Diseases > Cerebrovascular Disorders > Vascular Diseases > Cardiovascular Diseases > Medical Subject Headings (MeSH) Dementia, Vascular > Intracranial Arteriosclerosis > Cerebral Arterial Diseases > Intracranial Arterial Diseases > Cerebrovascular Disorders > Vascular Diseases > Cardiovascular Diseases > Medical Subject Headings (MeSH) Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Dementia, Vascular > Dementia > Delirium, Dementia, Amnestic, Cognitive Disorders > Mental Disorders > Medical Subject Headings (MeSH) Cerebral Arterial Diseases > Cerebrovascular Disorders > Brain Diseases > Central Nervous System Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Dementia, Vascular > Intracranial Arteriosclerosis > Cerebral Arterial Diseases > Cerebrovascular Disorders > Brain Diseases > Central Nervous System Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Dementia, Vascular > Cerebrovascular Disorders > Brain Diseases > Central Nervous System Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Cerebral Arterial Diseases > Intracranial Arterial Diseases > Cerebrovascular Disorders > Brain Diseases > Central Nervous System Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Dementia, Vascular > Intracranial Arteriosclerosis > Cerebral Arterial Diseases > Intracranial Arterial Diseases > Cerebrovascular Disorders > Brain Diseases > Central Nervous System Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Dementia, Vascular > Dementia > Brain Diseases > Central Nervous System Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) X
History note:	Cerebrovascular Disorders (1994-2004) \| Dementia, Multi-Infarct (1994-2004)X
historyNote*:	2005; use DEMENTIA, MULTI-INFARCT 2000-2004 X
publicMeSHNote*:	2005; see DEMENTIA, MULTI-INFARCT 2000-2004 X
Scope note:	A familial, cerebral arteriopathy mapped to chromosome 19q12, and characterized by the presence of granular deposits in small CEREBRAL ARTERIES producing ischemic STROKE; PSEUDOBULBAR PALSY; and multiple subcortical infarcts (CEREBRAL INFARCTION). CADASIL is an acronym for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. CADASIL differs from BINSWANGER DISEASE by the presence of MIGRAINE WITH AURA and usually by the lack of history of arterial HYPERTENSION. (From Bradley et al, Neurology in Clinical Practice, 2000, p1146) X
activeMeSHYear*:	2006 \| 2007X
dateCreated*:	2004-07-07X
dateEstablished*:	2005-01-01X
dateRevised*:	2005-06-30X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	agsX
Type:	Concept X
Coordinate terms:	Dementia, Multi-Infarct \| Cerebral Amyloid Angiopathy \| Infarction, Anterior Cerebral Artery \| Infarction, Middle Cerebral Artery \| Infarction, Posterior Cerebral Artery \| Intracranial Aneurysm \| Intracranial Arteriosclerosis \| Moyamoya Disease \| Adrenal Hyperplasia, Congenital \| Anemia, Hemolytic, Congenital \| Anemia, Hypoplastic, Congenital \| Ataxia Telangiectasia \| Blood Coagulation Disorders, Inherited \| Brugada Syndrome \| Camurati-Engelmann Syndrome \| Cardiomyopathy, Hypertrophic, Familial \| Cherubism \| Chromosome Disorders \| Cystic Fibrosis \| Dwarfism \| Eye Diseases, Hereditary \| Familial Mediterranean Fever \| Genetic Diseases, X-Linked \| Genetic Diseases, Y-Linked \| Hajdu-Cheney Syndrome \| Hemoglobinopathies \| Heredodegenerative Disorders, Nervous System \| Hyperthyroxinemia, Familial Dysalbuminemic \| Jervell-Lange Nielsen Syndrome \| Kallmann Syndrome \| Kartagener Syndrome \| Marfan Syndrome \| Metabolism, Inborn Errors \| Muscular Dystrophies \| Myasthenic Syndromes, Congenital \| Nail-Patella Syndrome \| Neoplastic Syndromes, Hereditary \| Osteogenesis Imperfecta \| Pain Insensitivity, Congenital \| Romano-Ward Syndrome \| Skin Diseases, Genetic \| Werner Syndrome X
URI:	X
Labels and equivalent concepts:	Cerebral autosomal dominant arteriopati (sv, replaced) Ärfltig vaskulär demens (sv, replaced) X
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